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从商陆有丝分裂原刺激的小鼠脾细胞条件培养基中纯化一种多能集落刺激因子。

Purification of a multipotential colony-stimulating factor from pokeweed mitogen-stimulated mouse spleen cell conditioned medium.

作者信息

Cutler R L, Metcalf D, Nicola N A, Johnson G R

出版信息

J Biol Chem. 1985 Jun 10;260(11):6579-87.

PMID:4039729
Abstract

A factor able to stimulate the proliferation and differentiation of multipotential stem cells and progenitor cells of the granulocyte-macrophage, eosinophil, and erythroid lineages as well as being able to maintain factor-dependent cell lines in culture has been purified from pokeweed mitogen-stimulated mouse spleen cell-conditioned medium. The factor was purified over 2 million-fold by sequential fractionation using salting out chromatography, chromatography on phenyl-Sepharose, gel filtration on Sephadex G-75, ion exchange chromatography on DEAE-Sepharose, reverse-phase high performance liquid chromatography on a phenyl-silica column, and gel permeation high performance liquid chromatography. All of the biological activities ascribed to the multipotential colony-stimulating factor co-fractionated through all steps, and the other known mouse-active hemopoietic regulator in pokeweed mitogen-stimulated mouse spleen cell-conditioned medium, granulocyte-macrophage colony-stimulating factor, was separated at the ion exchange step. Two protein species having Mr = 24,000 and 19,000 were visualized by silver-staining of sodium dodecyl sulfate-polyacrylamide gels of the purified factor. Both species migrated coincidently with the biological activities. The factor was active at a half-maximal concentration of 1 X 10(-13) M when assayed on a factor-dependent cell line.

摘要

一种能够刺激粒细胞-巨噬细胞、嗜酸性粒细胞和红系谱系的多能干细胞和祖细胞增殖与分化,并且能够在培养中维持依赖因子的细胞系的因子,已从商陆有丝分裂原刺激的小鼠脾细胞条件培养基中纯化出来。通过使用盐析色谱、苯基-琼脂糖色谱、Sephadex G-75凝胶过滤、DEAE-琼脂糖离子交换色谱、苯基硅胶柱反相高效液相色谱和凝胶渗透高效液相色谱进行顺序分级分离,该因子被纯化了超过200万倍。归因于多能集落刺激因子的所有生物活性在所有步骤中都共同分级分离,并且商陆有丝分裂原刺激的小鼠脾细胞条件培养基中另一种已知的对小鼠有活性的造血调节因子——粒细胞-巨噬细胞集落刺激因子,在离子交换步骤中被分离。通过对纯化因子的十二烷基硫酸钠-聚丙烯酰胺凝胶进行银染,可见两种分子量分别为24,000和19,000的蛋白质条带。这两种条带的迁移与生物活性一致。当在依赖因子的细胞系上进行测定时,该因子在半最大浓度为1×10⁻¹³ M时具有活性。

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